Chenopodium ambrosioides pollen
- Generic Name
- Chenopodium ambrosioides pollen
- Drug Type
- Biotech
- Unique Ingredient Identifier
- WIB701MW2H
Overview
Chenopodium ambrosioides pollen is the pollen of the Chenopodium ambrosioides plant. Chenopodium ambrosioides pollen is mainly used in allergenic testing.
Background
Chenopodium ambrosioides pollen is the pollen of the Chenopodium ambrosioides plant. Chenopodium ambrosioides pollen is mainly used in allergenic testing.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|
No clinical trials found
No clinical trials found for this drug
FDA Approved Products
Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 2009/11/13 | 49288-0153 | ||
SUBCUTANEOUS, INTRADERMAL | 10000 [PNU] in 1 mL | 2009/12/04 | 36987-3262 | ||
SUBCUTANEOUS, INTRADERMAL | 0.0167 g in 1 mL | 2009/11/13 | 49288-0085 | ||
SUBCUTANEOUS, INTRADERMAL | 0.05 g in 1 mL | 2009/12/04 | 36987-3267 | ||
SUBCUTANEOUS, INTRADERMAL | 40000 [PNU] in 1 mL | 2009/12/04 | 36987-3265 | ||
SUBCUTANEOUS, INTRADERMAL | 0.00167 g in 1 mL | 2009/12/02 | 49288-0660 | ||
SUBCUTANEOUS, INTRADERMAL | 0.1 g in 1 mL | 2009/12/04 | 36987-3268 | ||
SUBCUTANEOUS, INTRADERMAL | 20000 [PNU] in 1 mL | 2009/12/04 | 36987-3263 | ||
SUBCUTANEOUS, INTRADERMAL | 20000 [PNU] in 1 mL | 2009/12/04 | 36987-3264 | ||
SUBCUTANEOUS, INTRADERMAL | 10000 [PNU] in 1 mL | 2009/12/04 | 36987-3261 |
EMA Approved Products
Medicine Name | EMA Number | Auth. Holder | Country | Drug Type | Status | Issued | Opinion | Revision |
|---|
No EMA products found
No EMA products found for this drug
HSA Approved Products
Product Name | Manufacturer | Dosage Form | Strength | Approved | Approval No. |
|---|
No HSA products found
No HSA products found for this drug
NMPA Approved Products
Product Name | Approval No. | Manufacturer | Dosage Form | Trade Name | Strength | Type | Status | Date | Import |
|---|
No NMPA products found
No NMPA products found for this drug
PPB Approved Products
Product Name | Registration Code | Company | Category | Sale Type | Reg. Date |
|---|
No PPB products found
No PPB products found for this drug
TGA Approved Products
Product Name | ARTG ID | Sponsor | Status | Reg. Date | Ingredient |
|---|---|---|---|---|---|
319898 | Active | 2019/07/09 | Dysphania ambrosioides |
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